A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110906



Internal ID18905896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:88711382..88711447hg38UCSC Ensembl
Outerchr14:89177726..89177791hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961322
SamplesKWS1
Known GenesEML5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110906
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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